KEGG   Homo sapiens (human): 64919
Entry
64919             CDS       T01001                                 
Symbol
BCL11B, ATL1, ATL1-alpha, ATL1-beta, ATL1-delta, ATL1-gamma, CTIP-2, CTIP2, IDDFSTA, IMD49, RIT1, SMARCM2, ZNF856B, hRIT1-alpha
Name
(RefSeq) BCL11 transcription factor B
  KO
K22046  B-cell lymphoma/leukemia 11B
Organism
hsa  Homo sapiens (human)
Pathway
hsa05202  Transcriptional misregulation in cancer
Network
nt06240  Transcription (cancer)
  Element
N00144  TLX1 rearrangement to transcriptional repression
Disease
H00091  T-B+Severe combined immunodeficiency
H02463  Syndromic intellectual developmental disorder
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09160 Human Diseases
  09161 Cancer: overview
   05202 Transcriptional misregulation in cancer
    64919 (BCL11B)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03000 Transcription factors [BR:hsa03000]
    64919 (BCL11B)
Transcription factors [BR:hsa03000]
 Eukaryotic type
  Zinc finger
   Cys2His2 others
    64919 (BCL11B)
SSDB
Motif
Pfam: zf-C2H2 zf-C2H2_4 zf-H2C2_2 zf-H2C2_5 Actin_micro DUF3268
Other DBs
NCBI-GeneID: 64919
NCBI-ProteinID: NP_612808
OMIM: 606558
HGNC: 13222
Ensembl: ENSG00000127152
UniProt: Q9C0K0 L8B7P7
Position
14:complement(99169287..99272197)
AA seq 894 aa
MSRRKQGNPQHLSQRELITPEADHVEAAILEEDEGLEIEEPSGLGLMVGGPDPDLLTCGQ
CQMNFPLGDILVFIEHKRKQCGGSLGACYDKALDKDSPPPSSRSELRKVSEPVEIGIQVT
PDEDDHLLSPTKGICPKQENIAGPCRPAQLPAVAPIAASSHPHSSVITSPLRALGALPPC
LPLPCCSARPVSGDGTQGEGQTEAPFGCQCQLSGKDEPSSYICTTCKQPFNSAWFLLQHA
QNTHGFRIYLEPGPASSSLTPRLTIPPPLGPEAVAQSPLMNFLGDSNPFNLLRMTGPILR
DHPGFGEGRLPGTPPLFSPPPRHHLDPHRLSAEEMGLVAQHPSAFDRVMRLNPMAIDSPA
MDFSRRLRELAGNSSTPPPVSPGRGNPMHRLLNPFQPSPKSPFLSTPPLPPMPPGGTPPP
QPPAKSKSCEFCGKTFKFQSNLIVHRRSHTGEKPYKCQLCDHACSQASKLKRHMKTHMHK
AGSLAGRSDDGLSAASSPEPGTSELAGEGLKAADGDFRHHESDPSLGHEPEEEDEEEEEE
EEELLLENESRPESSFSMDSELSRNRENGGGGVPGVPGAGGGAAKALADEKALVLGKVME
NVGLGALPQYGELLADKQKRGAFLKRAAGGGDAGDDDDAGGCGDAGAGGAVNGRGGGFAP
GTEPFPGLFPRKPAPLPSPGLNSAAKRIKVEKDLELPPAALIPSENVYSQWLVGYAASRH
FMKDPFLGFTDARQSPFATSSEHSSENGSLRFSTPPGDLLDGGLSGRSGTASGGSTPHLG
GPGPGRPSSKEGRRSDTCEYCGKVFKNCSNLTVHRRSHTGERPYKCELCNYACAQSSKLT
RHMKTHGQIGKEVYRCDICQMPFSVYSTLEKHMKKWHGEHLLTNDVKIEQAERS
NT seq 2685 nt   +upstreamnt  +downstreamnt
atgtcccgccgcaaacagggcaacccgcagcacttgtcccagagggagctcatcacccca
gaggctgaccatgtggaggccgccatcctcgaagaagacgagggtctggagatagaggag
ccaagtggcctggggctgatggtgggtggccccgaccctgacctgctcacctgtggccag
tgtcaaatgaacttccccttgggggacatcctggtttttatagagcacaaaaggaagcag
tgtggcggcagcttgggtgcctgctatgacaaggccctggacaaggacagcccgccaccc
tcctcacgctccgagctcaggaaagtgtccgagccggtggagatcgggatccaagtcacc
cccgacgaagatgaccacctgctctcacccacgaaaggcatctgtcccaagcaggagaac
attgcagggccgtgcaggcctgcccagctgccagcggtggcccccatagctgcctcctcc
caccctcactcatccgtgatcacttcacctctgcgtgccctgggcgctctcccgccctgc
ctccccctgccgtgctgcagcgcgcgcccggtctcgggtgacgggactcagggtgagggt
cagacggaggctccctttggatgccagtgtcagttgtcaggtaaagatgagccttccagc
tacatttgcacaacatgcaagcagcccttcaacagcgcgtggttcctgctgcagcacgcg
cagaacacgcacggcttccgcatctacctggagcccgggccggccagcagctcgctcacg
ccgcggctcaccatcccgccgccgctcgggccggaggccgtggcgcagtccccgctcatg
aatttcctgggcgacagcaaccccttcaacctgctgcgcatgacgggccccatcctgcgg
gaccacccgggcttcggcgagggccgcctgccgggcacgccgcctctcttcagtcccccg
ccgcgccaccacctggacccgcaccgcctcagtgccgaggagatggggctcgtcgcccag
caccccagtgccttcgaccgagtcatgcgcctgaaccccatggccatcgactcgcccgcc
atggacttctcgcggcggctccgcgagctggcgggcaacagctccacgccgccgcccgtg
tccccgggccgcggcaaccctatgcaccggctcctgaaccccttccagcccagccccaag
tccccgttcctgagcacgccgccgctgccgcccatgccccctggcggcacgccgcccccg
cagccgccagccaagagcaagtcgtgcgagttctgcggcaagaccttcaagttccagagc
aatctcatcgtgcaccggcgcagtcacacgggcgagaagccctacaagtgccagctgtgc
gaccacgcgtgctcgcaggccagcaagctcaagcgccacatgaagacgcacatgcacaag
gccggctcgctggccggccgctccgacgacgggctctcggccgccagctcccccgagccc
ggcaccagcgagctggcgggcgagggcctcaaggcggccgacggtgacttccgccaccac
gagagcgacccgtcgctgggccacgagccggaggaggaggacgaggaggaggaggaggag
gaggaggagctgctactggagaacgagagccggcccgagtcgagcttcagcatggactcg
gagctgagccgcaaccgcgagaacggcggtggtggggtgcccggggtcccgggcgcgggg
ggcggcgcggccaaggcgctggctgacgagaaggcgctggtgctgggcaaggtcatggag
aacgtgggcctaggcgcactgccgcagtacggcgagctcctggccgacaagcagaagcgc
ggcgccttcctgaagcgtgcggcgggcggcggggacgcgggcgacgacgacgacgcgggc
ggctgcggggacgcgggcgcgggcggcgcggtcaacgggcgcgggggcggcttcgcgcca
ggcaccgagcccttccccgggctcttcccgcgcaagcccgcgccgctgcccagccccggg
ctcaacagcgccgccaagcgcatcaaggtggagaaggacctggagctgccgcccgccgcg
ctcatcccgtccgagaacgtgtactcgcagtggctggtgggctacgcggcgtcgcggcac
ttcatgaaggaccccttcctgggcttcacggacgcacgacagtcgcccttcgccacgtcg
tccgagcactcgtccgagaacggcagcctgcgcttctccacgccgcccggggacctgctg
gacggcggcctctcgggccgcagcggcacggccagcggaggcagcaccccgcacctgggc
ggcccgggccccgggcggcccagctccaaggagggccgccgcagcgacacgtgcgagtac
tgcggcaaggtgttcaagaactgcagcaacttgacggtgcaccggcggagccacaccggc
gagcggccttacaagtgcgagctgtgcaactacgcgtgcgcgcagagcagcaagctcacg
cgccacatgaagacgcacgggcagatcggcaaggaggtgtaccgctgcgacatctgccag
atgcccttcagcgtctacagcaccctggagaaacacatgaaaaagtggcacggcgagcac
ttgctgactaacgacgtcaaaatcgagcaggccgagaggagctaa

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Ontology (2)   
   KEGG BRITE (2)   
Pathway (1)   
   KEGG PATHWAY (1)   
Network (2)   
   KEGG NETWORK (2)   
Disease (5)   
   KEGG DISEASE (2)   
   OMIM (3)   
Genome (1)   
   KEGG GENOME (1)   
Gene (29)   
   KEGG ORTHOLOGY (1)   
   RefGene (23)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   OC (1)   
Protein sequence (11)   
   UniProt (2)   
   SWISS-PROT (1)   
   RefSeq(pep) (8)   
DNA sequence (22)   
   RefSeq(nuc) (8)   
   GenBank (7)   
   EMBL (7)   
Protein domain (6)   
   Pfam (6)   
All databases (79)   

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